Nickel Salts Research Articles

Rational fabrication of low carbon foot-print electrode materials for lithium-ion batteries from electric arc furnace dust via integrated hydrometallurgical process

Transforming industrial waste into high-value-added products represents a new avenue in the field of material science. This paper puts forward a comprehensive example for future works which target fabricating low-carbon footprint electrodes for rechargeable batteries. Within this scope, first time in the open literature, an integrated hydrometallurgical process has been designed to fabricate metal oxide powders of different properties from electric arc furnace (EAF) dust. Leaching, cementation, distillation, chemical precipitation, and calcination are used to produce powders rich in zinc oxide (Sample 1), ferrite (Sample 2), and nanocomposite (Sample 3) from the electric arc furnace flue dust.While sample 1 (zinc oxide with 97.8% purity) may be used in optics and other engineering applications, sample 2 (rich in zinc ferrite) and sample 3 (made of nanocomposites) that are recovered from the EAF dust may be utilized as electrode active material in lithium-ion batteries: Sample 2 and Sample 3 retain 43% and 50% of their capacities after 125th cycle, respectively. To further improve the cycle performance of Sample 2, the powder rich in ferrite is mixed with nickel salt, then heat treated. The latter performs 65% capacity retention after 125th cycle. The fact that every fabricated electrode achieves 125 cycles with success demonstrates the viability of the proposed technique; thus, various procedures may be developed to further elaborate the use of various industrial wastes in electrode fabrication.

Properties of Nickel Compose

This article has been to study nano-nickel (n-Ni) derivate production. Subject has been pursued formation of pure n-Ni and composed form of Ni under dimensional excuse. Anti-ferromagnetic nNi has been material of NaCl structure to confer p-type semi-conduction. Synthetic nickel nanoparticle has been produced by reduction of nickel salt in ethylene glycol (EG) in presence of sodium borohydride (NaBH4) as reducing agent. Preparation of NiO has been pursued either by heating above 400 °C or reaction of nickel powder with oxygen to give NiO or green nickel oxide formation by heating moistened nickel powder at 1000 °C, where subjective kinetic rate limitation has been dependent on addition of extraneous NiO.

Получение солей цветных металлов и железа из продуктов и отходов медно-никелевого производства

The article shows the possibility of producing non-ferrous metal and iron salts from intermediate products and waste of copper-nickel production in JSC "Kola MMC". Technological schemes and examples of methods for obtaining pure cobalt, nickel and iron salts using liquid extraction methods are given.

Monodispersed NiO Nanoparticles into SBA-15: An Efficient Nanocatalyst to Produce Ketone-Alcohol (KA) Oil by the Oxidation of Cyclohexane in Mild Conditions

A simple and efficient approach to preparing highly efficient and reusable NiO@SBA-15 nanocatalysts for the oxidation of cyclohexane to produce ketone-alcohol (KA) oil was reported. These nanocatalysts were prepared by the dispersion of NiO NPs into SBA-15 using a coordination-assisted grafting method. In this approach, four commercially available nickel salts were immobilized into amino-functionalized SBA-15. After washing and calcination, four new nanocatalysts were obtained. The high dispersion of NiO NPs into SBA-15 was confirmed by HR-TEM and XRD. Different oxidants such as O2, H2O2, t-butyl hydrogen peroxide (TBHP), and meta-Chloroperoxybenzoic acid (m-CPBA) were evaluated. However, m-CPBA exhibited the highest catalytic activity. Compared to different catalysts reported in the literature, for the first time, 75–99% of cyclohexane was converted to KA oil over NiO@SBA-15. In addition, the cyclohexane conversion and K/A ratio were affected by the reaction time, catalyst dose, Ni content, and NiO dispersion. Moreover, NiO@SBA-15 maintained a high catalytic activity during five successive cycles.

Novel Antioxidants Based on Selected 3d Metal Coordination Compounds with 2-Hydroxybenzaldehyde 4,S-Diallylisothiosemicarbazone.

2-Hydroxybenzaldehyde 4,S-diallylisothiosemicarbazone (HL) was synthesized and characterized by 1H, 13C NMR and FTIR spectroscopies. It exists in solution in two isomeric forms: cis (~25%) and trans (~75%). Six stable complexes were obtained by interaction of HL with copper(II), nickel(II), cobalt(III) and iron(III) salts: [Cu(L)Cl] (1), [Cu(L)NO3] (2), [Cu(3,4-Lut)(L)NO3] (3), [Ni(L)OAc] (4), [Co(L)2]Cl (5), [Fe(L)2]NO3 (6). The synthesized complexes have been studied by elemental analysis, FTIR, molar electrical conductivity and single crystal X-ray diffraction (6). For all compounds the antioxidant activity against cation radicals ABTS•+ was studied. All complexes and free ligand are more active than trolox that is used in medicine practice. Complex 4 (IC50=7.20µM) is the most active one. The introduction of heterocyclic amine did not improve the antioxidant activity. The introduction of S-allyl group into isothiosemicarbazone affected the activity of the synthesized substances, and in some cases the resulting complexes exhibit greater activity than complexes with isothiosemicarbazones with other S-radicals.

Whole genome expression analysis of trembling aspen (Populus tremuloides) genotypes exposed to increasing concentrations of nickel

Excess metals in the soil are a known type of abiotic stress and many plant species have evolved specific metal resistance mechanisms to cope and avoid or reduce toxicity symptoms. Studies on P. tremuloides genetic response to nickel are limited. This present study aims to 1) Assess gene expression dynamics in P. tremuloides seedlings treated with varying concentrations of nickel salts and, 2) Compare gene expression profiles among the different treatment groups. Trembling aspen (Populus tremuloides) seedlings were treated with varying concentrations of nickel nitrates (150 mg Ni / 1 kg of dry soil, 800 mg / kg, and 1, 600 mg / kg). The whole genome expression was analyzed using Illumina sequencing. Overall, 52,987 genes were identified from which 36,770 genes were selected as differently expressed. In general, there was an increase in number of differentially expressed genes as the nickel concentration increased when compared to water. The number of downregulated (439–600) and upregulated (123–560) genes increases with the nickel concentration increase. A detailed analysis suggested that the 800 mg / kg nickel concentration is the threshold at which an early abiotic stress response may be triggered as seen by the highly upregulated LEA protein and two calcium binding proteins when compared to water. For the highest nickel concentration, 7-deoxyloganetin glucosyltransferase was highly upregulated while an auxin response factor, Flavonol 3-sulfotransferase, and a predicted ABC transporter family protein were downregulated. The heatmap showed that the genes were grouped into six clusters based on the changes in expression as nickel concentration increased. The cluster of genes that had increased gene expression with increasing nickel concentration also had multiple enriched Gene ontology (GO) terms related to heavy metal and abiotic stress including metal ion transport, antioxidant activity, photosynthesis, and ribosomal activity. GO terms that decreased in expression with increasing nickel concentrations include ATP and ADP binding, protein kinase activity, integral component of membrane, protein phosphorylation and transmembrane transport.

Carbon-Supported Nickel Catalysts—Comparison in Alpha-Pinene Oxidation Activity

In this work, carbon-supported nickel catalysts with different Ni content (1, 2.5, 5, 10, and 20 wt%) were tested in the oxidation of alpha-pinene in solvent-free reaction conditions. The process of catalyst preparation consisted of two stages. In the first stage, the activated carbon from spent coffee grounds was obtained. In the second stage, the active phase in the form of nickel compounds was applied using two methods: (1) the impregnation of the material with the nickel salt solution, and next reduction in H2, and (2) the hydrothermal method in the autoclave using the reductor and the reaction stabilizer. The obtained catalysts were subjected to the following instrumental studies: FT-IR, XRD, SEM, and N2 adsorption at −196 °C. The performed catalytic tests showed that the catalysts containing 5 wt% of Ni (porous material obtained by the impregnation method) and 1 wt% of Ni (porous material obtained by the hydrothermal method) were the most active in the oxidation of alpha-pinene, and the main oxidation products were alpha-pinene oxide, verbenol, and verbenone. Ultimately, the hydrothermal method of catalyst preparation turned out to be more advantageous because it allows one to obtain higher selectivities of the epoxide compound, probably due to the greater stability of this organic compound in pores.

A Comparative Study: Adsorption Behavior of Different Nickel (II) Salts on to Alkaline Soil

A Comparative Study: Adsorption Behavior of Different Nickel (II) Salts on to Alkaline Soil

In situ transmogrification of nanoarchitectured Fe-MOFs decorated porous carbon nanofibers into efficient positrode for asymmetric supercapacitor application

In situ transmogrification is one of the most promising ways to synthesize positrode materials using a chemical treatment approach under optimal conditions for supercapacitor applications. The nickel salt concentration plays a vital role in the complete transmogrification of Fe-MOFs@PCNFs into Ni-Fe-OH@PCNFs (positrode). Herein, we successfully transform the tetragonal Fe-MOFs@PCNFs structure into pellet-like Ni-Fe-OH@PCNFs via in situ transmogrification under fixed temperature and pressure. The obtained Ni-Fe-OH@PCNFs-1 possess a unique porous architecture with a large surface area (74.3 m2g−1), which facilitates ion relocation and electron movement within the materials during charging/discharging. Owing to the limited surface area of electroactive materials, the double transition metal hydroxides (Ni-Fe-OH@PCNFs-D) synthesized directly (i.e., by employing two metal salts instantaneously) suffer a rapid decline in capacitance during cyclic stability test. The Ni-Fe-OH@PCNFs-1 electrode generated from Fe-MOFs@PCNFs has excellent cycling stability with ~86.7% capacitance retention and ~ 91.3% coulombic efficiency after 10,000 cycles at 10 A g−1. It also exhibits a remarkable specific capacitance of 1528 F g−1 at 1 A g−1. Additionally, the asymmetric supercapacitors (Ni-Fe-OH@PCNFs-1//Fe2O3/NPC@PCNFs) exhibit a maximum energy density of 44.3 Wh kg−1 at a power density of 907 W kg−1). The results of this work suggest the possibility of using MOF-derived nanoporous electrode materials and additional transition metal hydroxides for supercapacitors.

Nickel-Catalyzed Direct Cross-Coupling of Aryl Thioether with Aryl Bromide.

A straightforward cross-coupling of aryl thioether with aryl bromide with the aid of nickel salt, magnesium, and lithium chloride in tetrahydrofuran at ambient temperature was accomplished. The one-pot reactions proceeded efficiently via C-S bond cleavage to produce the desired biaryls in modest to good yields, avoiding the use of pregenerated or commercial organometallic reagents.

Electrochemical Formation of Li-M-(Mʹ)-Si Phases Using Multivalent Electrolyte Salt Additives

Lithium-rich silicides (Li15Si4), formed during the electrochemical lithiation of silicon, show high reactivity with electrolyte components that contribute to capacity decay, formal lithium loss, and low coulombic efficiency. Recently, the reactivity of lithium silicides was found to be suppressed by substituting a multivalent cation (i.e. Mg, Ca) for lithium that results in the room temperature formation of a ternary Li-M-Si phase. In this study, we explored a range of multivalent electrolyte salt additives (M = Ni, Cu, La, Ce, Sr, Ba, and Ca-Mg mixed salt) in a lithium-ion cell configuration and identified a room temperature electrochemical route to the formation of new ternary and quaternary lithium silicides. Using this method, both nickel and copper salts were found to plate onto the silicon electrode surface upon lithiation. Based on refined synchrotron XRD data, multivalent cations with an ionic radius similar to Na (∼1.03 Å) or smaller can be inserted electrochemically into a formally cation-deficient Li15Si4 host lattice to form new ternary (or quartenary) phases. The electrochemical synthesis of a new quaternary Li-M-M’-Si phase represents a facile route to preparing and scaling materials isostructural to the Heusler phase and electron-precise Li14MgSi4 phase that results in enhanced cycling and calendar life performance.

Crystal Growth and Crystal Structures of Gold(V) Compounds: Cu(AuF6)2, Ag(AuF6)2, and O2(CuF)3(AuF6)4 ⋅ HF

AbstractCrystal growth from anhydrous hydrogen fluoride solutions of M2+(M=Cu, Ag) and [AuF6]−gave M(AuF6)2salts (M=Cu, Ag). Similar attempts to prepare single crystals of the corresponding nickel, zinc and magnesium salts failed. The crystal structure of Cu(AuF6)2consists of layers of Cu2+cations connected by [AuF6]−anions, thus forming slabs. Only van der Waals interactions exist between adjacent slabs. The crystal structure of Ag(AuF6)2consists of a three‐dimensional framework in which Ag+cations are linked by [AuF6]−anions. Both structures are members of the MII(XVF6)2family, in which seven different structure types have been observed to date. In the crystal structure of O2(CuF)3(AuF6)4 ⋅ HF, the bridging AuF6units connect [−Cu−F−Cu−F−]∞chains to form stacks between which O2+cations and HF molecules are located.

Machine‐Learning Classification for the Prediction of Catalytic Activity of Organic Photosensitizers in the Nickel(II)‐Salt‐Induced Synthesis of Phenols

AbstractCatalytic systems using a small amount of organic photosensitizer for the activation of an inorganic (on‐demand ligand‐free) nickel(II) salt represent a cost‐effective method for cross‐coupling reactions, while C(sp2)−O bond formation remains less developed. Herein, we report a strategy for the synthesis of phenols with a nickel(II) salt and an organic photosensitizer, which was identified via an investigation into the catalytic activity of 60 organic photosensitizers consisting of various electron donor and acceptor moieties. To examine the effect of multiple intractable parameters on the catalytic activity of photosensitizers, machine‐learning (ML) models were developed, wherein we embedded descriptors representing their physical and structural properties, which were obtained from DFT calculations and RDKit, respectively. The study clarified that integrating both DFT‐ and RDKit‐derived descriptors in ML models balances higher “precision” and “recall” across a wide range of search space relative to using only one of the two descriptor sets.

Machine-Learning Classification for the Prediction of Catalytic Activity of Organic Photosensitizers in the Nickel(II)-Salt-Induced Synthesis of Phenols.

Catalytic systems using a small amount of organic photosensitizer for the activation of an inorganic (on-demand ligand-free) nickel(II) salt represent a cost-effective method for cross-coupling reactions, while C(sp2 )-O bond formation remains less developed. Herein, we report a strategy for the synthesis of phenols with a nickel(II) salt and an organic photosensitizer, which was identified via an investigation into the catalytic activity of 60 organic photosensitizers consisting of various electron donor and acceptor moieties. To examine the effect of multiple intractable parameters on the catalytic activity of photosensitizers, machine-learning (ML) models were developed, wherein we embedded descriptors representing their physical and structural properties, which were obtained from DFT calculations and RDKit, respectively. The study clarified that integrating both DFT- and RDKit-derived descriptors in ML models balances higher "precision" and "recall" across a wide range of search space relative to using only one of the two descriptor sets.

What are the Tower's method products: Metal-hydroxides or metal-glycerolates?

It has been long believed that colloidal nickel hydroxide nanoparticles are produced by the reaction of nickel salts, glycerol and potassium hydroxide known as the Tower method. In the present work, we challenge this belief and reveal the reasons for error in identification of nickel products produced by the Tower method. We propose that Ni-based precursor complexes are the primary products of the Tower method reaction, and these precursors undergo transition to layered Ni-glycerolate derivatives upon thermal treatment. We demonstrated the presence of Ni2+ coordinated to different types of O-donor ligands (glycerol, glycerolate ion, acetate ion and/or OH−) forming Ni-complex precursors. Using in-situ transmission electron microscopy, we showed that Ni-based precursor complexes can be converted to nickel nanoparticles upon exposure to electron beam, but no evidence of nickel hydroxide nanoparticle formation was found. The nickel hydroxide nanoparticles are only formed upon further reaction of Ni-glycerolate precursors with an aqueous alkaline solution. Those new findings shed light on the nature of the metal derivatives obtained by the reaction of Ni2+ and glycerol in the Tower method and provide more solid foundation to design electrode materials for batteries, supercapacitors, electrocatalysts and electrochemical sensors.

Catalytic Hydrodeoxygenation of Vanillin, a Bio-Oil Model Compound over Renewable Ni/Biochar Catalyst

This study aims to examine the hydrodeoxygenation (HDO) of vanillin, an oxygenated phenolic compound present in bio-oil, into creosol. Biochar residue generated when wood is slowly pyrolyzed is utilized as a catalyst support. To improve biochar’s physicochemical properties, H2SO4 (sulfuric acid) and KOH (potassium hydroxide) are used as chemical activators. By means of a wet impregnation method with nickel salt, an Ni/biochar catalyst was prepared and utilized in the HDO of vanillin using a 100 mL Parr reactor, catalyst loading 0.4–0.8 g, temperature 100 °C to 150 °C, hydrogen (H2) pressures of 30 to 50 bar, and a stirring rate of 1000 rpm. The prepared catalysts were characterized with the nitrogen-sorption isotherm technique, carbon dioxide temperature-programmed desorption (CO2-TPD), scanning electron microscopy (SEM) coupled with energy dispersed X-ray analysis (EDX), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR). Based on chemical treatment, Ni/biochar (KOH) pore sizes were found to be dominated by mesopores, with a surface area increase of 64.7% and a volume increase of 65.3%, while Ni/biochar (H2SO4) was mostly microporous and mesoporous, with an area increase of 372.3% and a volume increase of 256.8% in comparison to Ni/biochar (74.84 m2g−1 and 0.095 cm3g−1). Vanillin conversion of up to 97% with 91.17% selectivity to p-creosol was obtained over Ni/biochar catalyst; in addition to being highly selective and active for p-creosol, a plausible fuel, the catalyst was stable after four cycles. Chemical treatments of the biochar support resulted in improved physicochemical properties, leading to improved catalytic performance in terms of vanillin conversion and p-creosol yield in the order Ni/biochar (H2SO4) > Ni/biochar (KOH) > Ni/biochar.

Analysis and Comparison of Bio-Oils Obtained by Hydrothermal Liquefaction of Organic Waste

This paper presents an analysis of bio-oil quality depending on the type of input biomass, the process conditions and the catalytic systems used. Analysis of various catalytic system choices showed the prospects of using nickel and iron metal salts as homogeneous catalysts given that their use provided increases of 24.5% and 22.2%, respectively, in the yield of light-boiling bio-oil fractions (with a boiling point of up to 350 °C). Composition analysis of the bio-oils carried out using gas chromatography and nuclear magnetic resonance spectroscopy showed that fatty acids are the predominant group of substances in bio-oils produced from sewage sludge. Bio-oil synthesized from bark and wood waste contains phenolic alcohols and a limited range of cyclic hydrocarbons as the main components. In bio-oil produced from macroalgae, oxygen and nitrogen compounds of the piperazinedione and amides type are predominant. The sulfur and nitrogen content in all types of bio-oils is at an acceptable level. The results allow researchers to assert that organic waste processing enables production of sufficiently high-quality fuel, which can then be jointly processed with natural oil. Bio-oil produced from secondary sludge has the best quality, characterized by a high content of low-weight aliphatic compounds (with a boiling point of up to 350 °C), along with insignificant levels of nitrogen, sulfur and oxygen.

ВЛИЯНИЕ СЕРПЕНТИНИТА НА БРОНХО-ЛЕГОЧНУЮ СИСТЕМУ КРЫС

Attempts to use serpentinite in agriculture as a soil ameliorant led to the need to study its effect on living organisms. For this, serpentinite from the Kabardino-Balkarian deposit was added to the food for Westar rats. Taking serpentinite led to inflammatory-destructive changes both in the bronchi and lung parenchyma of rats, as well as to the restructuring of blood vessels with the formation of hypertension in the pulmonary circulation. Khabaz serpentinite contains nickel salts. Perhaps nickel had a damaging effect on the broncho-pulmonary system of rats. For the sake of safety for living objects, it is necessary to clean the rock from nickel salts and continue research.

Разработка технологического процесса фрикционного алитирования

Finishing anti-friction non-abrasive treatment (FANT) is one of the highly eff ective methods of increasing tribotechnical properties of parts (wear resistance and scoring resistance). The lack of highly eff ective technological media and devices for treating parts, as well as low corrosion resistance of the applied copper-containing coatings restrains the use of FANT. The technology of friction alitising, proposed by the authors, consists in the application of an aluminum-containing protective coating by friction, through the use of an aluminum rubbing tool and the developed technological medium, which includes aluminum salts. The technical alloy of AD1 grade GOST 4784-97, consisting of 99.3% Al, Fe - 0.3%; Si - up to 0.3%; Ti - not more than 0.15%; Zn - up to 0.1%; Mg - not more than 0.05%; Cu - up to 0.05%; manganese Mn - not more than 0.025% and impurities - up to 0.05% was chosen as a material of the rubbing tool. Cylindrical samples were used as the treated part during the elaboration. The technological medium developed by the authors includes salts of copper, tin and nickel, glycerine, glucose and water with additional content of aluminum salts. It has been established that qualitative friction alitising should be carried out in 3 to 4 passes at a sliding speed of the rubbing tool of 0.1 to 0.3 m/s and pressure of the rubbing tool within 5 to 7 MPa. For mass production, the technological process of alitising should include the following operations: cleaning before processing, defecting, friction alitising, cleaning after processing, quality control of coating and preservation of the part - if necessary for long storage.

Water-soluble nickel and iron salts for hydroxymethylfurfural (HMF) and water oxidation: the simplest precatalysts?

We report on a rapid, green, and cost-effective fabrication of nickel(-iron) oxyhydroxides by drop-coating and reconstructing water-soluble nitrate precursors, and their application for the OER and the oxidation of 5-hydroxymethylfurfural (HMF).